A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9607n54



Internal ID22777502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:14581657..14582392hg38UCSC Ensembl
chr5:14581766..14582501hg19UCSC Ensembl
chr5:14634766..14635501hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38736
hg19736
hg18736
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv597249, nsv597252, nsv597245
Samples
Known GenesFAM105A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9607n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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